Exam 12: The Chromosomal Basis of Inheritance
Exam 1: Introduction: Evolution and the Foundations of Biology36 Questions
Exam 2: The Chemical Context of Life137 Questions
Exam 3: Carbon and the Molecular Diversity of Life136 Questions
Exam 4: A Tour of the Cell75 Questions
Exam 5: Membrane Transport and Cell Signaling97 Questions
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Exam 9: The Cell Cycle56 Questions
Exam 10: Meiosis and Sexual Life Cycles62 Questions
Exam 11: Mendel and the Gene Idea63 Questions
Exam 12: The Chromosomal Basis of Inheritance46 Questions
Exam 13: The Molecular Basis of Inheritance67 Questions
Exam 14: Gene Expression: From Gene to Protein80 Questions
Exam 15: Regulation of Gene Expression50 Questions
Exam 16: Development, Stem Cells, and Cancer34 Questions
Exam 17: Viruses35 Questions
Exam 18: Genomes and Their Evolution29 Questions
Exam 19: Descent With Modification55 Questions
Exam 20: Phylogeny60 Questions
Exam 21: The Evolution of Populations70 Questions
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Exam 23: Broad Patterns of Evolution45 Questions
Exam 24: Early Life and the Diversification of Prokaryotes88 Questions
Exam 25: The Origin and Diversification of Eukaryotes71 Questions
Exam 26: The Colonization of Land by Plants and Fungi126 Questions
Exam 27: The Rise of Animal Diversity88 Questions
Exam 28: Plant Structure and Growth59 Questions
Exam 29: Resource Acquisition, Nutrition, and Transport in Vascular Plants110 Questions
Exam 30: Reproduction and Domestication of Flowering Plants67 Questions
Exam 31: Plant Responses to Internal and External Signals75 Questions
Exam 32: Homeostasis and Endocrine Signaling120 Questions
Exam 33: Animal Nutrition67 Questions
Exam 34: Circulation and Gas Exchange88 Questions
Exam 35: The Immune System91 Questions
Exam 36: Reproduction and Development118 Questions
Exam 37: Neurons, Synapses, and Signaling76 Questions
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Exam 39: Motor Mechanisms and Behavior79 Questions
Exam 40: Population Ecology and the Distribution of Organisms93 Questions
Exam 41: Species Interactions60 Questions
Exam 42: Ecosystems and Energy90 Questions
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Please use the following information to answer the question(s) below.
A man who is an achondroplastic dwarf with normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplastic dwarfism is autosomal dominant, and red-green color blindness is X-linked recessive.
-How many of the couple's daughters might be expected to be color-blind dwarfs?
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Correct Answer:
B
One possible result of chromosomal breakage is for a fragment to join a nonhomologous chromosome. What is this alteration called?
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Correct Answer:
D
Sex determination in mammals is due to the SRY gene on the Y chromosome. An abnormality of this region could allow which of the following to have a male phenotype?
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Correct Answer:
B
Figure 12.2
In a series of mapping experiments, the recombination frequencies for four different linked genes of Drosophila were determined as shown in Figure 12.2. What is the order of these genes on a chromosome map?

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Which of the following events causes recombination between linked genes to occur?
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Sturtevant provided genetic evidence for the existence of four pairs of chromosomes in Drosophila in which of the following ways?
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Cinnabar eyes is a sex-linked recessive characteristic in fruit flies. If a female having cinnabar eyes is crossed with a wild-type male, what percentage of the F1 males will have cinnabar eyes?
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Which of the following statements correctly describes aneuploid conditions?
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At what point in cell division is a chromosome lost so that, after fertilization with a normal gamete, the result is an embryo with 45,X?
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A phenotypically normal prospective couple seeks genetic counseling because the man knows that he has a translocation of a portion of his chromosome 4 that has been exchanged with a portion of his chromosome 12. Although he is normal because his translocation is balanced, he and his wife want to know the probability that his sperm will be abnormal. What is your prognosis regarding his sperm?
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A woman is found to have 47 chromosomes, including three X chromosomes. Which of the following describes her expected phenotype?
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Please use the following information to answer the question(s) below.
A man who is an achondroplastic dwarf with normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplastic dwarfism is autosomal dominant, and red-green color blindness is X-linked recessive.
-What proportion of their sons would be color-blind and of normal height?
(Multiple Choice)
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Of the following human aneuploidies, which is the one that generally has the most severe impact on the health of the individual?
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One map unit is equivalent to which of the following values?
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Abnormal chromosomes are frequently found in malignant tumors. Errors such as translocations may place a gene in close proximity to different control regions. Which of the following might then occur to make the cancer worse?
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How would one explain a testcross involving F1 dihybrid flies in which more parental-type offspring than recombinant-type offspring are produced?
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Which of the following statements best describes the SRY gene?
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Why does recombination between linked genes continue to occur?
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Red-green color blindness is a sex-linked recessive trait in humans. Two people with normal color vision have a color-blind son. What are the genotypes of the parents?
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Please use the following information to answer the question(s) below.
A plantlike organism on the planet Pandora can have three recessive genetic traits: bluish leaves, due to an allele (a) of gene A; a feathered stem, due to an allele (b) of gene B; and hollow roots due to an allele (c) of gene C. The three genes are linked and recombine.
A geneticist did a testcross with an organism that had been found to be heterozygous for the three recessive traits and was able to identify progeny of the phenotypic distribution (+ = wild type) shown in Figure 12.3.
Figure 12.3
-If recombination frequency is equal to distance in map units, what is the approximate distance between genes A and B?

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